Issue 58, 2016

Cyclopentadiene-mediated hydride transfer from rhodium complexes

Abstract

Attempts to generate a proposed rhodium hydride catalytic intermediate instead resulted in isolation of (Cp*H)Rh(bpy)Cl (1), a pentamethylcyclopentadiene complex, formed by C–H bond-forming reductive elimination from the fleeting rhodium hydride. The hydride transfer ability of diene 1 was explored through thermochemistry and hydride transfer reactions, including the reduction of NAD+.

Graphical abstract: Cyclopentadiene-mediated hydride transfer from rhodium complexes

Supplementary files

Article information

Article type
Communication
Submitted
20 jan 2016
Accepted
29 feb 2016
First published
01 mar 2016
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2016,52, 9105-9108

Cyclopentadiene-mediated hydride transfer from rhodium complexes

C. L. Pitman, O. N. L. Finster and A. J. M. Miller, Chem. Commun., 2016, 52, 9105 DOI: 10.1039/C6CC00575F

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